PKP1

plakophilin 1
OMIM: 601975, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green PKP1 in Desmosomal disorders


Level 2: Dermatological disorders
Version 0.33

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ectodermal dysplasia/skin fragility syndrome, MIM# 604536

Green PKP1 in Epidermolysis bullosa


Level 2: Dermatological disorders
Version 1.15

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ectodermal dysplasia/skin fragility syndrome, MIM# 604536

Green PKP1 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ectodermal dysplasia/skin fragility syndrome, MIM# 604536

Green PKP1 in Palmoplantar Keratoderma and Erythrokeratoderma


Level 2: Dermatological disorders
Version 0.132

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ectodermal dysplasia/skin fragility syndrome (MIM#604536)

Green PKP1 in Ectodermal Dysplasia


Level 2: Dermatological disorders
Version 0.86

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Ectodermal dysplasia/skin fragility syndrome MIM#604536